NP-MRD: Showing NP-Card for (2e,4e)-5-[(1s,2s,4ar,6s,7r,8s,8as)-7-hydroxy-6-(hydroxymethyl)-2,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-2-methylpenta-2,4-dienoic acid (NP0286368)

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Record Information

Version

2.0

Created at

2022-09-09 14:54:44 UTC

Updated at

2022-09-09 14:54:44 UTC

NP-MRD ID

NP0286368

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e,4e)-5-[(1s,2s,4ar,6s,7r,8s,8as)-7-hydroxy-6-(hydroxymethyl)-2,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-2-methylpenta-2,4-dienoic acid

Description

Tricodermic acid A, also known as tricodermate a, belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms. (2e,4e)-5-[(1s,2s,4ar,6s,7r,8s,8as)-7-hydroxy-6-(hydroxymethyl)-2,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-2-methylpenta-2,4-dienoic acid is found in Trichoderma spirale. Based on a literature review very few articles have been published on Tricodermic acid A.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 52  0  0  0  0  0  0  0  0999 V2000
    4.8802    0.3397    0.7571 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6198    1.0776   -0.5224 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4441    0.8912   -1.0855 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4748    0.0078   -0.4683 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2783   -0.2265   -0.9754 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2441   -1.0971   -0.4237 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6171   -1.7852    0.8568 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7496   -2.7448    0.7299 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7823   -0.7974    1.9782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2603    0.0139    2.1452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4013   -0.1525    1.2447 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4066    0.9670    1.3320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6116    0.6493    0.5235 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4050    1.9514    0.3506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7913    2.4743    1.5659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3193    0.1402   -0.8607 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4868   -0.5397   -1.2850 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1996   -0.8425   -0.9235 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9261   -1.2063   -2.3456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9980   -0.2724   -0.2069 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6405    1.9440   -1.0777 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7283    2.0737   -0.4933 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3964    2.6168   -2.2491 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1101    0.5553    1.5028 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8040   -0.7418    0.4953 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8743    0.6093    1.1672 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1813    1.3843   -2.0040 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7102   -0.4983    0.4516 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0477    0.2883   -1.9027 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0164   -1.8856   -1.1685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2909   -2.3902    1.1542 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4204   -3.8211    0.8377 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2329   -2.7275   -0.2918 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5274   -2.6295    1.5354 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6671   -0.7472    2.5964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2483    0.7546    2.9140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9304   -1.0914    1.5059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9700    1.9299    0.9922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7191    1.0361    2.4039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2818   -0.0310    1.0980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6967    2.6707   -0.1185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2411    1.8156   -0.3605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2593    1.7777    2.1107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2058    0.9852   -1.5760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7124   -1.1796   -0.5619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5196   -1.7514   -0.3528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8950   -1.1927   -2.9075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6001   -2.2813   -2.3720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1464   -0.6203   -2.8342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8723    0.7655   -0.5847 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9477    3.5339   -2.2972 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 13 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20  6  1  0
  6  5  1  0
  5  4  2  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2 21  1  0
 21 23  1  0
 21 22  2  0
  6  7  1  0
 20 11  1  0
  8 32  1  0
  8 33  1  0
  8 34  1  0
  7 31  1  1
  9 35  1  0
 10 36  1  0
 11 37  1  1
 12 38  1  0
 12 39  1  0
 13 40  1  1
 14 41  1  0
 14 42  1  0
 15 43  1  0
 16 44  1  6
 17 45  1  0
 18 46  1  1
 19 47  1  0
 19 48  1  0
 19 49  1  0
 20 50  1  6
  6 30  1  6
  5 29  1  0
  4 28  1  0
  3 27  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
 23 51  1  0
M  END


  Mrv1652309092216542D          

 23 24  0  0  1  0            999 V2000
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
 20 18  1  6  0  0  0
 11 20  1  0  0  0  0
  6 20  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0286368

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1C=C[C@H]2C[C@@H](CO)[C@H](O)[C@@H](C)[C@@H]2[C@H]1\C=C\C=C(/C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H28O4/c1-11-7-8-14-9-15(10-20)18(21)13(3)17(14)16(11)6-4-5-12(2)19(22)23/h4-8,11,13-18,20-21H,9-10H2,1-3H3,(H,22,23)/b6-4+,12-5+/t11-,13-,14-,15-,16-,17-,18+/m0/s1

> <INCHI_KEY>
HOZHXCYISCFSFQ-PFVFAAEOSA-N

> <FORMULA>
C19H28O4

> <MOLECULAR_WEIGHT>
320.429

> <EXACT_MASS>
320.198759382

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
36.892609010198726

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E,4E)-5-[(1S,2S,4aR,6S,7R,8S,8aS)-7-hydroxy-6-(hydroxymethyl)-2,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-2-methylpenta-2,4-dienoic acid

> <JCHEM_LOGP>
2.3165685993333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.552251010268645

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.772888019513712

> <JCHEM_PKA_STRONGEST_BASIC>
-2.628742037317294

> <JCHEM_POLAR_SURFACE_AREA>
77.76

> <JCHEM_REFRACTIVITY>
93.3958

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2E,4E)-5-[(1S,2S,4aR,6S,7R,8S,8aS)-7-hydroxy-6-(hydroxymethyl)-2,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-2-methylpenta-2,4-dienoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.334 -10.010   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -1.334 -10.010   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   20                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   20                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   13   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   11    6                                                  
CONECT   21    2   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol

Synonyms

Value	Source
Tricodermate a	Generator

Chemical Formula

C₁₉H₂₈O₄

Average Mass

320.4290 Da

Monoisotopic Mass

320.19876 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H]1C=C[C@H]2C[C@@H](CO)[C@H](O)[C@@H](C)[C@@H]2[C@H]1\C=C\C=C(/C)C(O)=O

InChI Identifier

InChI=1S/C19H28O4/c1-11-7-8-14-9-15(10-20)18(21)13(3)17(14)16(11)6-4-5-12(2)19(22)23/h4-8,11,13-18,20-21H,9-10H2,1-3H3,(H,22,23)/b6-4+,12-5+/t11-,13-,14-,15-,16-,17-,18+/m0/s1

InChI Key

HOZHXCYISCFSFQ-PFVFAAEOSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Trichoderma spirale	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Medium-chain fatty acids

Alternative Parents

Substituents

Medium-chain fatty acid
Branched fatty acid
Hydroxy fatty acid
Methyl-branched fatty acid
Unsaturated fatty acid
Cyclic alcohol
Secondary alcohol
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organic oxygen compound
Organooxygen compound
Primary alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

28289837

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101583709

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2e,4e)-5-[(1s,2s,4ar,6s,7r,8s,8as)-7-hydroxy-6-(hydroxymethyl)-2,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-2-methylpenta-2,4-dienoic acid (NP0286368)

MOL for NP0286368 ((2e,4e)-5-[(1s,2s,4ar,6s,7r,8s,8as)-7-hydroxy-6-(hydroxymethyl)-2,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-2-methylpenta-2,4-dienoic acid)

3D MOL for NP0286368 ((2e,4e)-5-[(1s,2s,4ar,6s,7r,8s,8as)-7-hydroxy-6-(hydroxymethyl)-2,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-2-methylpenta-2,4-dienoic acid)

3D SDF for NP0286368 ((2e,4e)-5-[(1s,2s,4ar,6s,7r,8s,8as)-7-hydroxy-6-(hydroxymethyl)-2,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-2-methylpenta-2,4-dienoic acid)

3D-SDF for NP0286368 ((2e,4e)-5-[(1s,2s,4ar,6s,7r,8s,8as)-7-hydroxy-6-(hydroxymethyl)-2,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-2-methylpenta-2,4-dienoic acid)

PDB for NP0286368 ((2e,4e)-5-[(1s,2s,4ar,6s,7r,8s,8as)-7-hydroxy-6-(hydroxymethyl)-2,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-2-methylpenta-2,4-dienoic acid)

3D PDB for NP0286368 ((2e,4e)-5-[(1s,2s,4ar,6s,7r,8s,8as)-7-hydroxy-6-(hydroxymethyl)-2,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-2-methylpenta-2,4-dienoic acid)

SMILES for NP0286368 ((2e,4e)-5-[(1s,2s,4ar,6s,7r,8s,8as)-7-hydroxy-6-(hydroxymethyl)-2,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-2-methylpenta-2,4-dienoic acid)

INCHI for NP0286368 ((2e,4e)-5-[(1s,2s,4ar,6s,7r,8s,8as)-7-hydroxy-6-(hydroxymethyl)-2,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-2-methylpenta-2,4-dienoic acid)

Structure for NP0286368 ((2e,4e)-5-[(1s,2s,4ar,6s,7r,8s,8as)-7-hydroxy-6-(hydroxymethyl)-2,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-2-methylpenta-2,4-dienoic acid)

3D Structure for NP0286368 ((2e,4e)-5-[(1s,2s,4ar,6s,7r,8s,8as)-7-hydroxy-6-(hydroxymethyl)-2,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-2-methylpenta-2,4-dienoic acid)